Literature DB >> 28577967

The underexplored question of β-amyloid monomers.

Agata Copani1.   

Abstract

Conceived more than 25 years ago, the amyloid cascade hypothesis of Alzheimer's disease has evolved to accommodate new findings, namely different forms of β-amyloid aggregates and downstream dysfunctions. Yet, the cascade does not mention its very beginning, the β-amyloid monomer. Here, I will discuss the monomer from a functional evolutionary perspective, highlighting the potential advantages of a native unfolded state that, however, involves an amyloidogenic risk. Finally, I will make a summary of what is known about its functional role in the brain and discuss the implications of its conceivable shortage in the development of Alzheimer's disease.
Copyright © 2017 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Aβ monomer; Brain hypometabolism; Glut3; IGF-IR; Neuronal glucose uptake; Neuroprotection

Mesh:

Substances:

Year:  2017        PMID: 28577967     DOI: 10.1016/j.ejphar.2017.05.057

Source DB:  PubMed          Journal:  Eur J Pharmacol        ISSN: 0014-2999            Impact factor:   4.432


  9 in total

Review 1.  Yeast red pigment, protein aggregates, and amyloidoses: a review.

Authors:  Olga V Nevzglyadova; Ekaterina V Mikhailova; Tonu R Soidla
Journal:  Cell Tissue Res       Date:  2022-03-08       Impact factor: 5.249

2.  Interaction of Amyloidogenic Proteins with Membranes and Molecular Mechanism for the Development of Alzheimer's disease.

Authors:  S Banerjee; Y L Lyubchenko
Journal:  Alzheimers Res Ther Open Access       Date:  2019-06-06

3.  Amyloid B-Protein Aggregation at Physiologically Relevant Concentrations. A Critical Role of Membranes.

Authors:  Y L Lyubchenko
Journal:  Alzheimers Res Ther Open Access       Date:  2020-10-28

4.  The Beta Amyloid Dysfunction (BAD) Hypothesis for Alzheimer's Disease.

Authors:  Heinz Hillen
Journal:  Front Neurosci       Date:  2019-11-07       Impact factor: 4.677

5.  Aβ Beyond the AD Pathology: Exploring the Structural Response of Membranes Exposed to Nascent Aβ Peptide.

Authors:  Valeria Rondelli; Mario Salmona; Laura Colombo; Giovanna Fragneto; Giulia C Fadda; Laura Cantu'; Elena Del Favero
Journal:  Int J Mol Sci       Date:  2020-11-05       Impact factor: 5.923

Review 6.  Conformational Essentials Responsible for Neurotoxicity of Aβ42 Aggregates Revealed by Antibodies against Oligomeric Aβ42.

Authors:  Chuli Song; Tianyu Zhang; Yingjiu Zhang
Journal:  Molecules       Date:  2022-10-10       Impact factor: 4.927

Review 7.  Structural Studies Providing Insights into Production and Conformational Behavior of Amyloid-β Peptide Associated with Alzheimer's Disease Development.

Authors:  Anatoly S Urban; Konstantin V Pavlov; Anna V Kamynina; Ivan S Okhrimenko; Alexander S Arseniev; Eduard V Bocharov
Journal:  Molecules       Date:  2021-05-13       Impact factor: 4.411

8.  Interaction of Aβ42 with Membranes Triggers the Self-Assembly into Oligomers.

Authors:  Siddhartha Banerjee; Mohtadin Hashemi; Karen Zagorski; Yuri L Lyubchenko
Journal:  Int J Mol Sci       Date:  2020-02-08       Impact factor: 5.923

9.  β-amyloid monomers drive up neuronal aerobic glycolysis in response to energy stressors.

Authors:  Rosa Santangelo; Maria Laura Giuffrida; Cristina Satriano; Marianna Flora Tomasello; Stefania Zimbone; Agata Copani
Journal:  Aging (Albany NY)       Date:  2021-07-21       Impact factor: 5.682

  9 in total

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